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通过转座子诱变鉴定 Hydrogenophaga sp. PBC 中 4-氨基苯磺酸盐降解途径相关基因。

Identification of genes involved in the 4-aminobenzenesulfonate degradation pathway of Hydrogenophaga sp. PBC via transposon mutagenesis.

机构信息

Department of Biological Sciences, Faculty of Biosciences and Bioengineering, Universiti Teknologi Malaysia, Johor, Malaysia.

出版信息

FEMS Microbiol Lett. 2011 May;318(2):108-14. doi: 10.1111/j.1574-6968.2011.02245.x. Epub 2011 Mar 8.

DOI:10.1111/j.1574-6968.2011.02245.x
PMID:21323982
Abstract

Genes involved in the 4-aminobenzenesulfonate (4-ABS) degradation pathway of Hydrogenophaga sp. PBC were identified using transposon mutagenesis. The screening of 10,000 mutants for incomplete 4-ABS biotransformation identified four mutants with single transposon insertion. Genes with insertions that impaired the ability to utilize 4-ABS for growth included (1) 4-sulfocatechol 1,2-dioxygenase β-subunit (pcaH2) and 3-sulfomuconate cycloisomerase involved in the modified β-ketoadipate pathway; (2) 4-aminobenzenesulfonate 3,4-dioxygenase component (sadA) involved in aromatic ring hydroxylation; and (3) transposase gene homolog with a putative cis-diol dehydrogenase gene located downstream. The pcaH2 mutant strain accumulated brown metabolite during growth on 4-ABS which was identified as 4-sulfocatechol through thin layer chromatography and HPLC analyses. Supplementation of wild-type sadA gene in trans restored the 4-ABS degradation ability of the sadA mutant, thus supporting the annotation of its disrupted gene.

摘要

利用转座子突变技术鉴定了氢噬菌属 PBC 中 4-氨基苯磺酸盐(4-ABS)降解途径相关的基因。对 10000 个不完全 4-ABS 生物转化突变体进行筛选,发现了 4 个带有单个转座子插入的突变体。插入导致丧失利用 4-ABS 进行生长能力的基因包括(1)参与修饰的β-酮己二酸途径的 4-磺基儿茶酚 1,2-双加氧酶β亚基(pcaH2)和 3-磺基戊二酸环异构酶;(2)参与芳香环羟化的 4-氨基苯磺酸盐 3,4-加双氧酶组分(sadA);和(3)位于下游的转座酶基因同源物和推定的顺式二醇脱氢酶基因。在 4-ABS 上生长时,pcaH2 突变株积累了棕色代谢物,通过薄层层析和 HPLC 分析鉴定为 4-磺基儿茶酚。野生型 sadA 基因的互补恢复了 sadA 突变体的 4-ABS 降解能力,因此支持其破坏基因的注释。

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